Sanofi, Bridgewater, New Jersey, USA.
Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
CPT Pharmacometrics Syst Pharmacol. 2021 Aug;10(8):941-952. doi: 10.1002/psp4.12667. Epub 2021 Jul 27.
A population pharmacokinetic model was developed using data from healthy subjects and patients with moderate-to-severe asthma receiving intravenous or subcutaneous dupilumab doses. A total of nine phase I to phase III studies were pooled (202 healthy subjects and 1912 patients with asthma including 68 adolescents) in the model development. The best model was a two-compartment model with parallel linear and nonlinear Michaelis-Menten elimination with first order absorption. The PK parameter estimates were distribution volume of central compartment 2.76 L, linear elimination rate 0.0418 1/day, and subcutaneous bioavailability 60.9%. Pharmacokinetics (PK) properties of dupilumab in patients with asthma were determined to be comparable to those of healthy subjects and patients with atopic dermatitis. Only body weight exerts a notable effect explaining between-subject variability in dupilumab PK, but dose adjustment for weight is not warranted based on results from clinical studies. There is no PK difference between adolescent and adult patients with asthma after correction for body weight.
建立了一个群体药代动力学模型,该模型使用了接受静脉或皮下注射度普利尤单抗的中重度哮喘患者和健康受试者的数据。在模型开发中,共有九项 I 期至 III 期研究进行了汇总(包括 68 名青少年在内的 202 名健康受试者和 1912 名哮喘患者)。最佳模型为具有平行线性和非线性米氏消除的两室模型,且具有一级吸收。PK 参数估计值为中央隔室分布容积 2.76 L,线性消除率 0.0418 1/天,皮下生物利用度 60.9%。在哮喘患者中,度普利尤单抗的药代动力学(PK)特性与健康受试者和特应性皮炎患者相似。只有体重对度普利尤单抗 PK 的个体间变异性有显著影响,但根据临床研究结果,体重调整剂量是没有必要的。在对体重进行校正后,青少年和成年哮喘患者之间在 PK 方面没有差异。